{{Rsnum
|rsid=80338867
|Chromosome=8
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=KIAA0196
|position=125056817
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KIAA0196
}}{{omim
|id=610657
|rsnum=80338867
|variant=0001
}}{{ClinVar
|rsid=80338867
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=126069059
|CHROM=8
|dbSNPBuildID=131
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=KIAA0196:9897
|GENE_NAME=KIAA0196
|GENE_ID=9897
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.126069059C>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1827; 610657.0001
|CLNSIG=5
|CLNCUI=C1863704; C1863704
|CLNDBN=Spastic paraplegia 8
|Disease=Spastic paraplegia 8
|CLNACC=RCV000001220.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1827:C1863704:603563:100989
}}{{PMID Auto
|PMID=17160902
|Title=Mutations in the KIAA0196 gene at the SPG8 locus cause hereditary spastic paraplegia.
|OA=1
}}